PL232108A1 - - Google Patents

Info

Publication number
PL232108A1
PL232108A1 PL23210881A PL23210881A PL232108A1 PL 232108 A1 PL232108 A1 PL 232108A1 PL 23210881 A PL23210881 A PL 23210881A PL 23210881 A PL23210881 A PL 23210881A PL 232108 A1 PL232108 A1 PL 232108A1
Authority
PL
Poland
Prior art keywords
sup
sub
group
groups containing
preparation
Prior art date
Application number
PL23210881A
Other versions
PL128513B1 (en
Original Assignee
Draco Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Draco Ab filed Critical Draco Ab
Publication of PL232108A1 publication Critical patent/PL232108A1/xx
Publication of PL128513B1 publication Critical patent/PL128513B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
    • C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
    • C07C215/34—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings containing hydroxy groups and carbon atoms of six-membered aromatic rings bound to the same carbon atom of the carbon skeleton and at least one hydroxy group bound to another carbon atom of the carbon skeleton
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/27—Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A61K31/375—Ascorbic acid, i.e. vitamin C; Salts thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Pulmonology (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Endocrinology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Saccharide Compounds (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Luminescent Compositions (AREA)
  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

New bronchospasmolytically active compounds exhibiting long duration of action and reduced undesired side effects of the structural formulaand therapeutically acceptable salts thereof, in which formula R is selected from the group consisting of -C(CH<sub>3</sub>)<sub>3</sub>,andR<sup>1</sup> is selected from the group consisting of H and <sub>R2</sub>, R<sup>2</sup> represents the radical of the formulawherein R<sup>3</sup> is selected from the group consisting of(a) H(b) alkyl groups containing 1-3 carbon atomswherein R<sup>5</sup> is selected from the group consisting of(a) OH(b) alkoxy groups containing 1-3 carbon atoms and whereinR<sup>4</sup> is selected from the group consisting of(a) H(b) alkyl groups containing 1-3 carbon atoms, with the proviso that R<sup>3</sup> and R<sup>4</sup> are combined as follows:processes for the preparation thereof, chemical intermediates at their preparation, pharmaceutical preparations containing them, and their medicinal use.
PL1981232108A 1980-07-09 1981-07-08 Method of obtaining new derivatives of 1-phenyl ethanol PL128513B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8022439 1980-07-09
GB8116441 1981-05-29

Publications (2)

Publication Number Publication Date
PL232108A1 true PL232108A1 (en) 1982-08-02
PL128513B1 PL128513B1 (en) 1984-02-29

Family

ID=26276161

Family Applications (1)

Application Number Title Priority Date Filing Date
PL1981232108A PL128513B1 (en) 1980-07-09 1981-07-08 Method of obtaining new derivatives of 1-phenyl ethanol

Country Status (29)

Country Link
US (2) US4419364A (en)
EP (1) EP0043807B1 (en)
KR (3) KR850000301B1 (en)
AT (1) ATE7689T1 (en)
AU (1) AU539976B2 (en)
CA (1) CA1180021A (en)
CS (1) CS221845B2 (en)
CY (1) CY1273A (en)
DD (1) DD202001A5 (en)
DE (1) DE3163871D1 (en)
DK (1) DK157678C (en)
ES (3) ES8300678A1 (en)
FI (1) FI73666C (en)
GR (1) GR74291B (en)
HK (1) HK5385A (en)
HU (2) HU184959B (en)
IE (1) IE51373B1 (en)
IS (1) IS1262B6 (en)
LU (1) LU88304I2 (en)
MX (1) MX9203239A (en)
MY (1) MY8700026A (en)
NO (2) NO152130C (en)
NZ (1) NZ197628A (en)
PH (2) PH16535A (en)
PL (1) PL128513B1 (en)
PT (1) PT73336B (en)
SG (1) SG79784G (en)
SU (1) SU1128830A3 (en)
YU (3) YU42116B (en)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8904064D0 (en) * 1989-12-01 1989-12-01 Astra Ab IMPROVED METHOD OF PREPARING AND INTERMEDIATE FOR THE MANUFACTURE OF BAMBUTEROL
SE9000948D0 (en) * 1990-03-16 1990-03-16 Draco Ab NEW USE
US5830422A (en) * 1995-06-23 1998-11-03 Ormiston Mining And Smelting Co. Ltd. Method for production of sodium bicarbonate, sodium carbonate and ammonium sulfate from sodium sulfate
EP0892639A4 (en) * 1996-01-29 1999-06-09 Savor Evelyn Method of treating undesired uterine contractions using optically pure r- or rr-isomers of adrenergic beta-2 agonists
SE9604752D0 (en) * 1996-12-20 1996-12-20 Astra Ab Formulation and use
KR20030085658A (en) * 2002-04-30 2003-11-07 한올제약주식회사 An improved synthetic method of bambuterol
EP1542672B1 (en) * 2002-08-08 2008-09-03 Wen Tan R-bambuterol, its preparation and therapeutic uses
US7495028B2 (en) * 2002-08-08 2009-02-24 Wen Tan R-bambuterol, its preparation and therapeutic uses
RU2387646C2 (en) * 2003-08-29 2010-04-27 Рэнбакси Лабораториз Лимитед Type iv phosphodiesterase inhibitors
US20070259874A1 (en) * 2003-11-26 2007-11-08 Palle Venkata P Phosphodiesterase Inhibitors
WO2006081986A1 (en) * 2005-02-07 2006-08-10 F.Hoffmann-La Roche Ag Bambuterol and integrin inhibitor combination
WO2007031838A1 (en) 2005-09-16 2007-03-22 Ranbaxy Laboratories Limited Substituted pyrazolo [3,4-b] pyridines as phosphodiesterase inhibitors
WO2007045979A1 (en) 2005-10-19 2007-04-26 Ranbaxy Laboratories Limited Pharmaceutical compositions of muscarinic receptor antagonists
AU2006305620A1 (en) * 2005-10-19 2007-04-26 Ranbaxy Laboratories Limited Compositions of phosphodiesterase type IV inhibitors
JO2868B1 (en) 2006-08-22 2015-03-15 رانبكسي لابوراتوريز ليمتد Matrix Metalloproteinase inhibitors
WO2008035316A2 (en) * 2006-09-22 2008-03-27 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
EA200900472A1 (en) * 2006-09-22 2009-10-30 Ранбакси Лабораторис Лимитед PHOSPHODESTERASE INHIBITORS IV TYPE
EP1958947A1 (en) 2007-02-15 2008-08-20 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type 4
US20110130403A1 (en) * 2007-03-14 2011-06-02 Ranbaxy Laboratories Limited Pyrazolo [3, 4-b] pyridine derivatives as phosphodiesterase inhibitors
SI2124944T1 (en) * 2007-03-14 2012-05-31 Ranbaxy Lab Ltd Pyrazolo?á3,4-b?åpyridine derivatives as phosphodiesterase inhibitors
EP2111861A1 (en) 2008-04-21 2009-10-28 Ranbaxy Laboratories Limited Compositions of phosphodiesterase type IV inhibitors
CN103119030A (en) 2010-07-30 2013-05-22 兰贝克赛实验室有限公司 Matrix metalloproteinase inhibitors
US20140148459A1 (en) 2010-09-24 2014-05-29 Ranbaxy Laboratories Limited Matrix metalloproteinase inhibitors
MY176727A (en) 2012-12-03 2020-08-20 Pfizer Selective androgen receptor modulators
US9784726B2 (en) 2013-01-08 2017-10-10 Atrogi Ab Screening method, a kit, a method of treatment and a compound for use in a method of treatment
CN104557614B (en) * 2014-12-15 2017-01-04 广东东阳光药业有限公司 A kind of method of reducing of amine
CN105622461B (en) * 2016-01-29 2018-06-19 华南理工大学 A kind of compound and its preparation method and application
CN105859589B (en) * 2016-04-05 2018-09-28 深圳市康立生生物科技有限公司 A method of preparing bambuterol impurity C
GB201714745D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
GB201714740D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
GB201714736D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
GB201714734D0 (en) 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
CN109942462B (en) * 2019-03-06 2022-01-14 宏冠生物药业有限公司 Synthesis process of bambuterol hydrochloride
GB201903832D0 (en) 2019-03-20 2019-05-01 Atrogi Ab New compounds and methods
GB202205895D0 (en) 2022-04-22 2022-06-08 Atrogi Ab New medical uses
CN117069620A (en) * 2022-05-17 2023-11-17 成都施贝康生物医药科技有限公司 A kind of phloroglucinol derivative and its preparation and use
CN120583945A (en) 2023-01-20 2025-09-02 阿托基公司 Beta2-adrenergic receptor agonists for the treatment or prevention of muscle wasting
GB202302225D0 (en) 2023-02-16 2023-04-05 Atrogi Ab New medical uses
GB202303229D0 (en) 2023-03-06 2023-04-19 Atrogi Ab New medical uses
CN117586152B (en) * 2023-11-23 2026-04-03 黑龙江乌苏里江制药有限公司 A method for preparing bambuterol hydrochloride
GB202403169D0 (en) 2024-03-05 2024-04-17 Atrogi Ab New medical uses
WO2025238248A1 (en) 2024-05-17 2025-11-20 Atrogi Ab USE OF β2-ADRENERGIC RECEPTOR AGONISTS IN TREATING MUSCLE WASTING
CN120585720A (en) * 2025-06-12 2025-09-05 肇庆学院 A nasal drug preparation for dual-target drugs and its application

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE178032C1 (en) 1961-01-01
DE1643488U (en) 1949-11-28 1952-09-11 G E Hilge Fa INCUBATOR.
DK85789C (en) 1955-07-05 1958-06-30 Cilag Ag Process for the preparation of d, 1- or 1-isopropyl-aminomethyl- (3,4-dihydroxy-phenyl) -carbinol or salts thereof.
DE1768167U (en) 1958-04-02 1958-06-04 Artur O Herrmann ROAD OBSTACLE WARNING DEVICE.
DE1275069B (en) 1960-02-15 1968-08-14 Boehringer Sohn Ingelheim 1- (3 ', 5'-dihydroxyphenyl) -1-hydroxy-2-isopropylaminoalkanes and processes for their preparation
BE622434A (en) 1961-09-14
FR1324857A (en) * 1962-06-14 1963-04-19 Chemie Linz Ag Process for the preparation of phenylethanolamine derivatives
GB1141606A (en) 1965-04-12 1969-01-29 Rech S Et D Applic Scient Et M Improvements in alkyl ethers of substituted phenylaminoethanols
DE1543372A1 (en) 1966-10-18 1971-04-01 Boehringer Sohn Ingelheim Process for the preparation of o-substituted 3,4-dioxyphenylalkanolamines
US3937838A (en) * 1966-10-19 1976-02-10 Aktiebolaget Draco Orally active bronchospasmolytic compounds and their preparation
SE358633B (en) 1966-10-19 1973-08-06 Draco Ab
NO132866C (en) 1966-10-19 1976-01-21 Draco Ab
SE335359B (en) 1966-10-19 1971-05-24 Draco Ab
FR6087M (en) 1967-01-10 1968-06-04
SE369299B (en) 1967-10-18 1974-08-19 Draco Ab
SE338324B (en) 1967-12-19 1971-09-06 Haessle Ab
NO129903B (en) 1969-04-01 1974-06-10 Sterling Drug Inc
AT294046B (en) 1969-07-08 1971-11-10 Chemie Linz Ag Process for the preparation of N, N'-bis [2- (3 ', 4'-dihydroxyphenyl) -2-hydroxyethyl] -hexamethylenediamine, its optically active forms and the salts thereof
US3657319A (en) * 1970-05-05 1972-04-18 Smith Kline French Lab Alpha-aminoalkyl-4-hydroxy-3-carboalkoxyaminobenzyl alcohols
NO126437B (en) 1970-08-05 1973-02-05 Draco Ab
NL7112938A (en) 1970-09-30 1972-04-05
CH550771A (en) 1970-10-30 1974-06-28 Hoffmann La Roche PROCESS FOR THE PRODUCTION OF PHENAETHYLAMINE DERIVATIVES.
US3876679A (en) 1970-12-09 1975-04-08 Aldrich Chem Co Inc Di-substituted phenethylcarbamic acid esters
FI55988C (en) 1971-10-19 1979-11-12 Klinge Co Chem Pharm Fab REFERENCE FOR THERAPEUTIC USE OF THERAPEUTIC THERAPEUTIC O-ACYLPHENOLETHANOLAMINER
US4011258A (en) 1973-06-21 1977-03-08 Aktiebolaget Draco Orally active bronchospasmolytic compounds
FI56673C (en) 1974-03-29 1981-02-04 Huhtamaeki Yhthymae Oy NYTT FOERFARANDE FOER FRAMSTAELLNING AV ALFA-TERT-BYTYLAMINOMETHYL-4-HYDROXY-M-XYLEN-ALFA1 ALFA3-DIOL
JPS556625B2 (en) 1974-05-16 1980-02-18
US4063025A (en) * 1975-02-05 1977-12-13 Yamanouchi Pharmaceutical Co., Ltd. 4-Substituted amino-α-aminomethylbenzyl alcohol derivatives
SE7510988L (en) 1975-10-01 1977-04-02 Draco Ab NEW PHARMACEUTICAL ACTIVE ASSOCIATIONS
DE2710997C3 (en) * 1977-03-14 1980-08-14 Dr. Karl Thomae Gmbh, 7950 Biberach 4-Alkoxy carbonylamino-phenylethanolamines, their production and their use as pharmaceuticals

Also Published As

Publication number Publication date
CA1180021A (en) 1984-12-27
LU88304I2 (en) 1994-05-04
YU43168B (en) 1989-04-30
ES8304534A1 (en) 1983-03-01
GR74291B (en) 1984-06-21
IE811522L (en) 1982-01-09
CS221845B2 (en) 1983-04-29
AU539976B2 (en) 1984-10-25
YU86483A (en) 1983-12-31
HU184959B (en) 1984-11-28
KR850002741A (en) 1985-05-15
DK303481A (en) 1982-01-10
KR850002740A (en) 1985-05-15
SU1128830A3 (en) 1984-12-07
PH16535A (en) 1983-11-10
FI812158L (en) 1982-01-10
FI73666B (en) 1987-07-31
YU42116B (en) 1988-04-30
US4451663A (en) 1984-05-29
ES513108A0 (en) 1983-02-16
IE51373B1 (en) 1986-12-10
ES503768A0 (en) 1982-11-01
EP0043807B1 (en) 1984-05-30
DK157678B (en) 1990-02-05
FI73666C (en) 1987-11-09
CY1273A (en) 1985-03-08
NZ197628A (en) 1985-07-12
YU170481A (en) 1983-12-31
SG79784G (en) 1985-04-26
NO152130B (en) 1985-04-29
HU187611B (en) 1986-02-28
US4419364A (en) 1983-12-06
KR850000301B1 (en) 1985-03-18
KR850000870B1 (en) 1985-06-22
HK5385A (en) 1985-01-25
PT73336A (en) 1981-08-01
YU43169B (en) 1989-04-30
DK157678C (en) 1990-06-18
IS1262B6 (en) 1987-03-27
PH19447A (en) 1986-04-18
PT73336B (en) 1983-09-01
IS2657A7 (en) 1982-01-10
NO1996008I1 (en) 1996-06-27
EP0043807A2 (en) 1982-01-13
AU7261881A (en) 1982-01-14
NO812311L (en) 1982-01-11
EP0043807A3 (en) 1982-09-22
ES8300678A1 (en) 1982-11-01
PL128513B1 (en) 1984-02-29
MX9203239A (en) 1992-07-01
KR830006174A (en) 1983-09-20
ATE7689T1 (en) 1984-06-15
MY8700026A (en) 1987-12-31
ES513109A0 (en) 1983-03-01
DE3163871D1 (en) 1984-07-05
NO152130C (en) 1985-08-07
YU86383A (en) 1983-12-31
DD202001A5 (en) 1983-08-24
KR850000871B1 (en) 1985-06-22
ES8304072A1 (en) 1983-02-16

Similar Documents

Publication Publication Date Title
AU539976B2 (en) Therapeutically active compounds
SE8303013L (en) B-GAMMA DIHYDROPOLYPRENYLAL ALCOHOL DERIVATIVE AND PHARMACEUTICAL COMPOSITION CONTAINING A POLYPRENYL SUBSTANCE
ES8802014A1 (en) Aminohydroxyalkylbenzene anti-obesity and/or anti-hyperglycaemic agents.
DE3477488D1 (en) Polymethoxybenzyl piperazine derivatives, processes for their preparation and pharmaceutical compositions containing said derivatives
ES8100249A1 (en) Novel hydroxamic acid compounds, method for preparation thereof and medicaments containing such compounds
JPS5271492A (en) Synthesis of 9-substituted-2-substituted thioadenines
GB8306040D0 (en) Dibenzocycloheptenylidene compounds
DE3175939D1 (en) Use of gamma-piperidino-butyrophenones for the preparation of medicaments for treating diarrhoea
JPS5219684A (en) Preparation of novel alpha-amino acid derivatives
ES485828A1 (en) Substituted pyridazines, their use and preparation and medicinal preparations containing them.